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Roche Molecular Systems, Inc. - MagNA Pure LC - Class 2 Recall
Roche Applied Science MagNA Pure LC Version 3.0. The MagNA Pure LC (version 3.0) is a sample preparation instrument that can be used with the LightCycler instrument for automated isolation of nucleic acids in various types of biological materials. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 7, 2012 Category: Medical Equipment Source Type: alerts

Omni Life Science - Omnilife Science Apex Knee System Modular Tibia Augment - Class 2 Recall
Omnilife Science Apex Knee System Modular Tibia Augment, Size 1 x 4mm Ref: KC-54010. The Apex Knee System is intended for use as a primary or revision total knee replacement. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 13, 2012 Category: Medical Equipment Source Type: alerts

Omni Life Science - Omnilife Science Apex Knee System Modular Tibia Augment - Class 2 Recall
Omnilife Science Apex Knee System Modular Tibia Augment, Size 3 x 4mm Ref: KC-54030. The Apex Knee System is intended for use as a primary or revision total knee replacement. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 13, 2012 Category: Medical Equipment Source Type: alerts

Omni Life Science - Omnilife Science Apex Knee System Modular Tibia Augment - Class 2 Recall
Omnilife Science Apex Knee System Modular Tibia Augment, Size 5 x 4mm Ref: KC-54050. The Apex Knee System is intended for use as a primary or revision total knee replacement. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 13, 2012 Category: Medical Equipment Source Type: alerts

Omni Life Science - Omnilife Science Apex Knee System Modular Tibia Augment - Class 2 Recall
Omnilife Science Apex Knee System Modular Tibia Augment, Size 4 x 4mm Ref: KC-54040. The Apex Knee System is intended for use as a primary or revision total knee replacement. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 13, 2012 Category: Medical Equipment Source Type: alerts

Omni Life Science - Omnilife Science Apex Knee System Modular Tibia Augment - Class 2 Recall
Omnilife Science Apex Knee System Modular Tibia Augment, Size 6 x 4mm Ref: KC-54060. The Apex Knee System is intended for use as a primary or revision total knee replacement. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 13, 2012 Category: Medical Equipment Source Type: alerts

Omni Life Science - Omnilife Science Apex Knee System Modular Tibia Augment - Class 2 Recall
Omnilife Science Apex Knee System Modular Tibia Augment, Size 2 x 4mm Ref: KC-54020. The Apex Knee System is intended for use as a primary or revision total knee replacement. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 13, 2012 Category: Medical Equipment Source Type: alerts

Ellman International, Inc. - Pelleve - Class 2 Recall
Pelleve Non-Ablative Wrinkle Treatment Handpiece Pelleve---Elegance through science---Contents: One (1) Pelleve Handpiece (Reusable)---Ellman, 3333 Royal Avenue, Oceanside, NY 11572-3625 USA--- Non-ablative treatment of mild to moderate facial wrinkles and rhytids for skin phototypes I-IV. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 17, 2012 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart AED, CardioVive AED, GE Responder AED, Nihon Kohden CardioLife AED - Class 1 Recall
Powerheart G3 Automated External Defibrillators (Non-Wearable) and include the following models: Powerheart 9300A, 9300E, 9300P, 9390A, 9390E; CardioVive 92532, 92533; Nihon-Kohden 9200G, 9231; and GE Responder 2019198, 2023440 AEDs. The Powerheart AED G3 is indicated for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. Post-resuscitation, if the victim is breathing, the AED should be left attached to allow for acquisition and detection of the ECG rhythm. If a shockable ventricular tachyarrhythmia recurs, the device will charge automatically and be able to...
Source: Medical Device Recalls - February 27, 2012 Category: Medical Equipment Source Type: alerts

Coopervision Inc. - AVAIRA (enfilcon A) Daily Wear Sphere Contact Lens - Class 1 Recall
AVAIRA AQUAFORM Comfort Science enfilcon A Daily Wear SPHERE Soft Contact Lenses (disposable), Rx only, STERILE --- CooperVision: Hamble, SO31 4RF, UK -- Scottsville, NY 14546 USA -- Juana Diaz, PR 00795 USA --- Device Listing # D033736. Packaged: 6 Soft Contact Lenses per unit carton or trial product 3 pack. AVAIRA (enfilcon A) SPHERE soft contact lenses are indicated for the correction of ametropia (myopia or hyperopia) in aphakic and non-aphakic persons with non-diseased eyes. The lenses may be worn by persons who exhibit astigmatism of 2.00 diopters or less that does not interfere with visual acuity. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 11, 2012 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart AED, G3, CardioVive AED, GE Responder AED, Nihon Kohden CardioLife AED - Class 2 Recall
Powerheart Automated External Defibrillator (AED), G3 is indicated for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. Post-resuscitation, if the victim is breathing, the AED should be left attached to allow for acquisition and detection of the ECG rhythm. If a shockable ventricular tachyarrhythmia recurs, the device will charge automatically and be able to deliver therapy. Model numbers: Powerheart 9300A, 9300C, 9300D, 9300E, 9300P, 9390A, 9390E, CardioVive 92532, 92533, NK 9200G, 9231, and Responder 2019198, 2023440. Brand names: Powerheart AED, G3, Ca...
Source: Medical Device Recalls - September 19, 2011 Category: Medical Equipment Source Type: alerts

Roche Diagnostics Operations, Inc. - MagNA Pure LightCycler - Class 2 Recall
MagNA Pure LC 2.0 (software version 1.1.23 and 1.1.24) Roche Diagnostics Operations, Inc. An automated instrument used for isolation of nucleic acids (DNA, total RNA, total viral nucleic acids) from different kinds of biological research sample material (whole blood, serum, blood cells, culture cells, tissue, bacteria, fungi) using the specially designed MagNA Pure LC kits, for the purpose of life science research only and automated filling of different kinds of PCR reaction vessels (LightCycler Capillaries, 96-well PCR plates, PCR tube strips) with PCR reaction mixes and template nucleic acid, or other reaction tubes for...
Source: Medical Device Recalls - August 29, 2011 Category: Medical Equipment Source Type: alerts

Roche Diagnostics Operations, Inc. - MagNA Pure LightCycler - Class 2 Recall
MagNA Pure LC 1.0 (software version 3.0.11). Roche Diagnostics Operations, Inc. An automated instrument used for isolation of nucleic acids (DNA, total RNA, total viral nucleic acids) from different kinds of biological research sample material (whole blood, serum, blood cells, culture cells, tissue, bacteria, fungi) using the specially designed MagNA Pure LC kits, for the purpose of life science research only and automated filling of different kinds of PCR reaction vessels (LightCycler Capillaries, 96-well PCR plates, PCR tube strips) with PCR reaction mixes and template nucleic acid, or other reaction tubes for the makin...
Source: Medical Device Recalls - August 29, 2011 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart AED, G2 - Class 2 Recall
Automated External Defibrillator (non-wearable). Model number 9200, 9200N, 9200DN, 9200RD, 9210N, 9210RD, and CardioVive 92530. The battery component is warranted for 5 years, and electrodes have a shelf life of 2 years. The Powerheart AED G2 and CardioVive 92530 are intended to acquire the ECG rhythm for the detection of, and to provide treatment for, ventricular tachyarrhythmias of patients who are at risk of sudden cardiac arrest. The device is intended to be used in medically supervised environments by trained personnel, in which patients are under the direct care of physicians and/or medical persons authorized by th...
Source: Medical Device Recalls - August 3, 2011 Category: Medical Equipment Source Type: alerts

Roche Diagnostics Operations, Inc. - MagNA Pure LC 2.0 Instrument - Class 2 Recall
MagNA Pure LC 2.0 Instrument, catalog number 05197686001, Roche Diagnostics, Indianapolis, IN MagNA Pure LC 2.0 instrument is a robotic instrument for automated isolation of nucleic acids (DNA, total RNA , total viral nucleic acids) from different kinds of biological research sample material (whole blood, serum, blood cells, culture cells, tissue, bacteria, fungi) using the specially designed MagNA Pure LC kits, for the purpose of life science research only and automated filling of different kinds of PCR reaction vessels (LightCycler Capillaries, 96 well PCR plates, PCR tube strips) with PCR reaction mixes and template n...
Source: Medical Device Recalls - March 14, 2011 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - GE Responder 2000 Defibrillator/Monitor - Class 2 Recall
GE Responder 2000 Defibrillator/Monitor, models 2025653, 2026109, and 2026114 that were manufactured between July 25, 2008 and October 2, 2009 by GE Healthcare. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 10, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart 9390E automated external defibrillator - Class 2 Recall
Cardiac Science Powerheart 9390A automated external defibrillator. This fully automatic model does not require the user to press a shock button in order for the device to deliver therapy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - June 21, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Treadmill models TM55, TM65, and CR60 (brand names include Quinton, Burdick, and Cardiac Science). - Class 2 Recall
Treadmill models TM55, TM65, and CR60 (brand names include Quinton, Burdick, and Cardiac Science). (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - June 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Automatic External Defibrillator (AED) - Class 2 Recall
Responder 2000 Defibrillator/Monitor Models: 2025653, 2026109, and 2026114. Intended use: The Responder 2000 is indicated for the termination of certain fatal arrhythmias, such as ventricular fibrillation and symptomatic ventricular tachycardia. Delivery of energy in the synchronized mode is a method for treating atrial fibrillation, atrial flutter, paroxysmal supraventricular tachycardia, and in relatively stable patients, ventricular tachycardia. The semi-automatic advisory mode is for use in cardiac arrest in patients of at least 8 years of age. The patient must be unconscious, pulseless, and not breathing spontaneousl...
Source: Medical Device Recalls since July 07, 2006 - May 26, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart, CardioVive, Nihon Kohden and/or Responder AED - Class 1 Recall
Cardiac Science, Automated External Defibrillator (AED) under the following brand names (with respective model numbers): Powerheart AED G3: 9300A, 9300C, 9300D, 9300E, 9300P, 9390A/E; CardioVive: 92532 and 92533; Nihon Kohden: 9200G, and 9231; and Responder: 2019198 and 2023440. Cardiac Science, Bothell, WA 98021. Indicated for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - April 27, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart AED - Class 2 Recall
Powerheart 9390E automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Brand name: Cardiac Science. Product name: Powerheart. Device Operation: Semi-automatic. Color: Yellow. Voice Prompt Level: Extensive.(Extensive voice prompts provide more detailed instruction on device use, pad placement and CPR performance, as compared to the basic prompts.) CPR Metronome: Yes. Rescue Ready Indicator: Yes. Text Display: Yes. ECG Display: No. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - April 6, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart AED - Class 2 Recall
Powerheart 9300P automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Brand name: Cardiac Science. Product name: Powerheart. Device Operation: Semi-automatic w/manual override. Color: Yellow. Voice Prompt Level: Basic. CPR Metronome: Yes. Rescue Ready Indicator: Yes. Text Display: Yes. ECG Display: Yes. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - April 6, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart AED - Class 2 Recall
Powerheart 9390A automated external defibrillator. This fully automatic model does not require the user to press a shock button in order for the device to deliver therapy (when appropriate). Brand name: Cardiac Science. Product name: Powerheart. Device Operation: Fully automatic. Color: Yellow. Voice Prompt Level: Extensive.(Extensive voice prompts provide more detailed instruction on device use, pad placement and CPR performance, as compared to the basic prompts.) CPR Metronome: Yes. Rescue Ready Indicator: Yes. Text Display: Yes. ECG Display: No. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - April 6, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Cardiovive AED - Class 2 Recall
Cardiovive 92532 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Brand name: Burdick. Product name: Cardiovive. Device Operation: Semi-automatic. Color: Blue. Voice Prompt Level: Basic. CPR Metronome: No. Rescue Ready Indicator: Yes. Text Display: Yes. ECG Display: No. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - April 6, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Responder AED - Class 2 Recall
Responder 2023440 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Brand name: GE. Product name: Responder. Device Operation: Semi-automatic w/manual override. Color: GE Gold. Voice Prompt Level: Basic. CPR Metronome: Yes. Rescue Ready Indicator: Yes. Text Display: Yes. ECG Display: Yes. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - April 6, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart AED - Class 2 Recall
Powerheart 9300A automated external defibrillator. This fully automatic model does not require the user to press a shock button in order for the device to deliver therapy (when appropriate). Brand name: Cardiac Science. Product name: Powerheart. Device Operation: Fully automatic. Color: Yellow. Voice Prompt Level: Basic. CPR Metronome: No. Rescue Ready Indicator: Yes. Text Display: Yes. ECG Display: No. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - April 6, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart AED - Class 2 Recall
Powerheart 9300E automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Brand name: Cardiac Science. Product name: Powerheart. Device Operation: Semi-automatic. Color: Yellow. Voice Prompt Level: Basic. CPR Metronome: No. Rescue Ready Indicator: Yes. Text Display: Yes. ECG Display: No. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - April 6, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Cardiovive 92533 automated external defibrillator - Class 1 Recall
Burdick Cardiovive 92533 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart 9390A automated external defibrillator - Class 1 Recall
Cardiac Science Powerheart 9390A automated external defibrillator. This fully automatic model does not require the user to press a shock button in order for the device to deliver therapy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Responder 2023440 automated external defibrillator - Class 1 Recall
GE Responder 2023440 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart 9300A automated external defibrillator - Class 1 Recall
Cardiac Science Powerheart 9300A automated external defibrillator. This fully automatic model does not require the user to press a shock button in order for the device to deliver therapy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart 9300E automated external defibrillator - Class 1 Recall
Cardiac Science Powerheart 9300E automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart 9390E automated external defibrillator - Class 1 Recall
Cardiac Science Powerheart 9390E automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Cardiovive 92531 automated external defibrillator - Class 1 Recall
Burdick Cardiovive 92531 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - CardioLife automated external defibrillator - Class 1 Recall
NK 9231 CardioLife automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Responder 2019198 automated external defibrillator - Class 1 Recall
GE Responder 2019198 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart 9300C automated external defibrillator - Class 1 Recall
Cardiac Science Powerheart 9300C automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - CardioLife automated external defibrillator - Class 1 Recall
NK 9200G. CardioLife automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart 9300D automated external defibrillator - Class 1 Recall
Cardiac Science Powerheart 9300D automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Powerheart 9300P automated external defibrillator - Class 1 Recall
Cardiac Science Powerheart 9300P automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Cardiac Science Corporation - Cardiovive 92532 automated external defibrillator - Class 1 Recall
Burdick Cardiovive 92532 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - March 4, 2010 Category: Medical Equipment Source Type: alerts

Omni Life Science - APEX Hip System Bipolar Head - Class 2 Recall
Apex Hip System Bipolar Head Bipolar Head, 28 mm ID, 54 mm OD Product Code: H3-82854. Intended for use in combination with an Apex Hip System femoral for uncemented primary or revision hemiarthroplasty of the hip. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 10, 2009 Category: Medical Equipment Source Type: alerts

Omni Life Science - APEX Hip System Bipolar Head - Class 2 Recall
Apex Hip System Bipolar Head Bipolar Head, 28 mm ID, 53 mm OD Product Code: H3-82853. Intended for use in combination with an Apex Hip System femoral for uncemented primary or revision hemiarthroplasty of the hip. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 10, 2009 Category: Medical Equipment Source Type: alerts

Omni Life Science - APEX Hip System Bipolar Head - Class 2 Recall
Apex Hip System Bipolar Head, 22.225mm ID, 43 mm OD Product Code: H3-82243. Intended for use in combination with an Apex Hip System femoral for uncemented primary or revision hemiarthroplasty of the hip. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 10, 2009 Category: Medical Equipment Source Type: alerts

Omni Life Science - APEX Hip System Bipolar Head - Class 2 Recall
Apex Hip System Bipolar Head, 22.225mm ID, 38 mm OD Product Code: H3-82238. Intended for use in combination with an Apex Hip System femoral for uncemented primary or revision hemiarthroplasty of the hip. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 10, 2009 Category: Medical Equipment Source Type: alerts

Omni Life Science - APEX Hip System Bipolar Head - Class 2 Recall
Apex Hip System Bipolar Head Bipolar Head, 28 mm ID, 51 mm OD Product Code: H3-82851. Intended for use in combination with an Apex Hip System femoral for uncemented primary or revision hemiarthroplasty of the hip. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 10, 2009 Category: Medical Equipment Source Type: alerts

Omni Life Science - APEX Hip System Bipolar Head - Class 2 Recall
Apex Hip System Bipolar Head Bipolar Head, 28 mm ID, 56 mm OD Product Code: H3-82856. Intended for use in combination with an Apex Hip System femoral for uncemented primary or revision hemiarthroplasty of the hip. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 10, 2009 Category: Medical Equipment Source Type: alerts

Omni Life Science - APEX Hip System Bipolar Head - Class 2 Recall
Apex Hip System Bipolar Head Bipolar Head, 28 mm ID, 59 mm OD Product Code: H3-82859. Intended for use in combination with an Apex Hip System femoral for uncemented primary or revision hemiarthroplasty of the hip. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 10, 2009 Category: Medical Equipment Source Type: alerts

Omni Life Science - APEX Hip System Bipolar Head - Class 2 Recall
Apex Hip System Bipolar Head Bipolar Head, 28 mm ID, 52 mm OD Product Code: H3-82852. Intended for use in combination with an Apex Hip System femoral for uncemented primary or revision hemiarthroplasty of the hip. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 10, 2009 Category: Medical Equipment Source Type: alerts

Omni Life Science - APEX Hip System Bipolar Head - Class 2 Recall
Apex Hip System Bipolar Head Bipolar Head, 28 mm ID, 57 mm OD Product Code: H3-82857. Intended for use in combination with an Apex Hip System femoral for uncemented primary or revision hemiarthroplasty of the hip. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 10, 2009 Category: Medical Equipment Source Type: alerts